A curated catalogue of human genomic structural variation




Variant Details

Variant: essv6885433



Internal ID10280195
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
Outerchr16:46403143..46408230hg19UCSC Ensembl
Cytoband16q11.2
Allele length
AssemblyAllele length
hg195088
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusS
Merged Variantsesv2714373, esv2714360
Supporting Variants
SamplesSSM095
Known Genes
MethodSequencing
AnalysisBreakdancer:4 times standard deviation,VariationHunter:4 times standard deviation and at least 3 supportting reads
PlatformIllumina HiSeq 2000
Comments
ReferenceWong_et_al_2012b
Pubmed ID23290073
Accession Number(s)essv6885433
Frequency
Sample Size96
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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